Table 2.
Treatment variable | Patients (n = 185) |
---|---|
Ceftaroline fosamil line of therapy, n (%) | |
1 | 50 (27.0) |
2 | 49 (26.5) |
3 | 46 (24.9) |
≥4 | 40 (21.5) |
Duration of treatment, days, median (range) | 7 (2–35) |
Time from admission to first dose, days, median (range) | 1.9 (0–36) |
Time from symptom onset to first dose, days, median (range) | 6 (0–38) |
Daily dose, mg, median (range) | 1200 (200–1800) |
Treatment type, n (%)a | |
Empirical | 138 (74.6) |
Definitive/specific | 41 (22.0) |
Monotherapy/combination therapy, n (%) | |
Monotherapy | 56 (30.3) |
Combination therapyb | 129 (69.7) |
Aminoglycoside | 3 (2.3) |
β-lactam | 8 (6.2) |
Carbapenem | 7 (5.4) |
Ceftriaxone | 5 (3.9) |
Cephalosporin | 1 (0.8) |
Glycopeptide | 5 (3.9) |
Macrolide | 2 (1.6) |
β-lactam/combination | 36 (27.9) |
Sulphonamide | 57 (44.2) |
Clindamycin | 5 (3.9) |
Other | 5 (3.9) |
Administration location, n (%) | |
ICU | 66 (35.7) |
General ward | 115 (62.2) |
At home | 1 (0.5) |
Medical clinic | 30 (16.2) |
a n = 179 (data not available for six patients).
b n = 99 (data not available for 30 patients).